Vaccination with a Recombinant H7 Hemagglutinin-Based Influenza Virus Vaccine Induces Broadly Reactive Antibodies in Humans

Author:

Stadlbauer Daniel12,Rajabhathor Arvind1,Amanat Fatima1,Kaplan Daniel1,Masud Abusaleh3,Treanor John J.4,Izikson Ruvim5,Cox Manon M.5,Nachbagauer Raffael1ORCID,Krammer Florian1ORCID

Affiliation:

1. Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA

2. Department of Biotechnology, University of Natural Resources and Life Sciences, Vienna, Austria

3. Center for Excellence in Youth Education, Icahn School of Medicine at Mount Sinai, New York, New York, USA

4. Department of Medicine, University of Rochester Medical Center, Rochester, New York, USA

5. Protein Sciences Corporation, Meriden, Connecticut, USA

Abstract

Zoonotic infections with high case fatality rates caused by avian H7N9 influenza viruses have been reported since early 2013 in China. Since then, the fifth wave of the H7N9 epidemic emerged in China, resulting in higher numbers of laboratory-confirmed cases than in previous years. Recently, H7N9 has started to antigenically drift and split into two new lineages, the Pearl River Delta and Yangtze River Delta clades, which do not match stockpiled H7 vaccines well. Humans are immunologically naive to these subtypes, and an H7N9 strain that acquires the capability of efficient human-to-human transmission poses a credible pandemic threat. Other characteristics of H7N9 are raising concerns as well, like its ability to bind to receptors in the human upper respiratory tract, the recent emergence of highly pathogenic variants, and the ability to quickly gain resistance to neuraminidase inhibitors. Therefore, developing and testing H7N9 vaccines constitutes a priority for pandemic preparedness.

Funder

BARDA

HHS | National Institutes of Health

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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